A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521556



Internal ID15448849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6641895..6676953hg38UCSC Ensembl
Innerchr9:6641895..6676953hg19UCSC Ensembl
Innerchr9:6631895..6666953hg18UCSC Ensembl
Innerchr9:6631895..6666953hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3835059
hg1935059
hg1835059
hg1735059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698172
Samples
Known GenesGLDC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521556
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer